Document Detail


Multiple epiphyseal dysplasia: a family study.
MedLine Citation:
PMID:  515629     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Three generations of a single family exhibited evidence of multiple epiphyseal dysplasia. The distribution of involvement was entirely consistent with an autosomal dominant mode of inheritance. The family was characterized by premature osteoarthrosis of the hips developing in adolescence or early adulthood. In most patients there were no obvious signs of an underlying anomaly and the diagnosis was not recognized for a long time. Eventual diagnosis of the disorder allowed easy genetic counselling.
Authors:
T Gibson; J Highton
Related Documents :
8236519 - Familial sick sinus syndrome in two siblings.
9279759 - Neurogenic chronic idiopathic intestinal pseudo-obstruction, patent ductus arteriosus, ...
11507589 - Patient with bardet-biedl syndrome presenting with nystagmus at fifteen months of age.
7137169 - Iron overload in hereditary spherocytosis: association with hla-linked hemochromatosis.
24565179 - Building additional complexity to in vitro-derived intestinal tissues.
19213659 - Unilateral progressive osseous heteroplasia.
22399449 - A nationwide survey on quality of life and associated factors of adults with high-funct...
8871989 - An assessment tool to identify panic disorder.
3879279 - Epidemiology of musculoskeletal disorders (complaints) and related disability in canada.
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Rheumatology and rehabilitation     Volume:  18     ISSN:  0300-3396     ISO Abbreviation:  Rheumatol Rehabil     Publication Date:  1979 Nov 
Date Detail:
Created Date:  1980-02-15     Completed Date:  1980-02-15     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0355004     Medline TA:  Rheumatol Rehabil     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  239-42     Citation Subset:  AIM; IM    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Aged
Arthrography
Child
Child, Preschool
Chondrodysplasia Punctata / genetics*,  radiography
Female
Femur Head / radiography
Humans
Male
Middle Aged
Pedigree

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  The use of scintigraphy in the diagnosis and management of traumatic foot lesions in ballet dancers.
Next Document:  Quality criteria in Mammography (author's transl)